Canonical Allele Identifier: CA2061217
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs774882233

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202519077_202519078del , CM000664.2:g.202519077_202519078del GRCh38
NC_000002.11:g.203383800_203383801del , CM000664.1:g.203383800_203383801del GRCh37
NC_000002.10:g.203092045_203092046del NCBI36
NG_009363.1:g.147751_147752del , LRG_712:g.147751_147752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.852+25_852+26del MANE Select ENSP00000363708.4:n.852+25_852+26del
ENST00000638587.1:c.783+25_783+26del ENSP00000491062.1:n.783+25_783+26del
ENST00000374574.2:c.852+25_852+26del ENSP00000363702.2:n.852+25_852+26del
ENST00000374580.8:c.852+25_852+26del ENSP00000363708.4:n.852+25_852+26del
NM_001204.6:c.852+25_852+26del , LRG_712t1:c.852+25_852+26del NP_001195.2:n.852+25_852+26del
XM_011511687.1:c.852+25_852+26del XP_011509989.1:n.852+25_852+26del
XM_011511688.1:c.852+25_852+26del XP_011509990.1:n.852+25_852+26del
NM_001204.7:c.852+25_852+26del MANE Select NP_001195.2:n.852+25_852+26del